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rs1064795734

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome5
Position177292107
GeneNSD1
is asnp
is mentioned by
dbSNPrs1064795734
dbSNP (old)rs1064795734
ClinGenrs1064795734
ebirs1064795734
HLIrs1064795734
Exacrs1064795734
Gnomadrs1064795734
Varsomers1064795734
Maprs1064795734
PheGenIrs1064795734
Biobankrs1064795734
1000 genomesrs1064795734
hgdprs1064795734
ensemblrs1064795734
gopubmedrs1064795734
geneviewrs1064795734
scholarrs1064795734
googlers1064795734
pharmgkbrs1064795734
gwascentralrs1064795734
openSNPrs1064795734
23andMers1064795734
23andMe allrs1064795734
SNPshotrs1064795734
SNPdbers1064795734
MSV3drs1064795734
GWAS Ctlgrs1064795734
Max Magnitude0
ClinVar
Risk rs1064795734(C;C)
Alt rs1064795734(C;C)
Reference Rs1064795734(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NSD1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.176719108T>C
CLNSRC
CLNACC RCV000484869.1,